Canonical Allele Identifier: CA235318189
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs547443466
gnomAD v2: 12-40591047-G-A
gnomAD v3: 12-40197245-G-A
gnomAD v4: 12-40197245-G-A
MyVariant Identifiers: chr12:g.40591047G>A (hg19) chr12:g.40197245G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40197245G>A , CM000674.2:g.40197245G>A GRCh38
NC_000012.11:g.40591047G>A , CM000674.1:g.40591047G>A GRCh37
NC_000012.10:g.38877314G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416796.5:c.-63+472G>A ENSP00000398726.1:n.-63+472G>A
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